Furoin - ≥96%(GC) , CAS No.552-86-3

CAS: 552-86-3 Cat. No.: F156650 Molecular Weight: 192.17 Beilstein Registry Number: 19(3/4)2543
AVAILABLE TO ORDER
GRADE & PURITY ≥96%(GC)
Synonyms
D78158 | DTXSID60862181 | 5-19-05-00551 (Beilstein Handbook Reference) | Furoin, 98% | SCHEMBL155225 | UNII-FP41RNB020 | 1,2-Bis(2-furyl)-2-hydroxyethanone | FT-0626584 | .alpha.-Furoin | 1,2-Di-furan-2-yl-2-hydroxy-ethanone | 2-FURYL(HYDROXY)METHYL 2-FUR
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
F156650-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$9.90
5g
F156650-5g
8
$22.90
25g
F156650-25g
10
$80.90
100g
F156650-100g
4
$296.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥96%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Furoin was used as fluorogenic reagent for the selective and sensitive liquid chromatographic determination of various guanidines.

Specifications

Synonyms
D78158 | DTXSID60862181 | 5-19-05-00551 (Beilstein Handbook Reference) | Furoin, 98% | SCHEMBL155225 | UNII-FP41RNB020 | 1, 2-Bis(2-furyl)-2-hydroxyethanone | FT-0626584 | .alpha.-Furoin | 1, 2-Di-furan-2-yl-2-hydroxy-ethanone | 2-FURYL(HYDROXY)METHYL 2-FUR
Specifications & Purity
≥96%(GC)
Storage
Room temperature
Shipped In
Normal
Purity
≥96%(GC)
Names and Identifiers
Pubchem Sid488181257
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181257
Canonical SmilesC1=COC(=C1)C(C(=O)C2=CC=CO2)O
IUPAC Name1,2-bis(furan-2-yl)-2-hydroxyethanone
InChIKeyMIJRFWVFNKQQDK-UHFFFAOYSA-N
INCHI1S/C10H8O4/c11-9(7-3-1-5-13-7)10(12)8-4-2-6-14-8/h1-6,9,11H
Isomeric SMILES C1=COC(=C1)C(C(=O)C2=CC=CO2)O
WGK Germany 3
RTECS KM5774095
Molecular Weight 192.17
Beilstein 19(3/4)2543
Reaxy-Rn 84251
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=84251&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree Nodes Ketones - Aryl ketones
Direct ParentAryl alkyl ketones
Alternative Parents Acyloins  Heteroaromatic compounds  Furans  Alpha-hydroxy ketones  Secondary alcohols  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Aryl alkyl ketone - Acyloin - Heteroaromatic compound - Furan - Alpha-hydroxy ketone - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Alcohol - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLB1 Tchem Beta-galactosidase (339 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CES2 Tchem Carboxylesterase 2 (583 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KMT2A Tchem Histone-lysine N-methyltransferase MLL (17327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeDateItem
J2112571Certificate of AnalysisJul 10, 2025 F156650
J2112572Certificate of AnalysisJul 10, 2025 F156650
J2112573Certificate of AnalysisJul 10, 2025 F156650
G2315092Certificate of AnalysisJul 22, 2023 F156650
K2205184Certificate of AnalysisNov 09, 2022 F156650
K2205186Certificate of AnalysisNov 09, 2022 F156650
K2205188Certificate of AnalysisNov 09, 2022 F156650
K2205218Certificate of AnalysisNov 09, 2022 F156650
Chemical and Physical Properties
Melt Point(°C)137.0 to 141.0 °C
Molecular Weight192.170 g/mol
XLogP30.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass192.042 Da
Monoisotopic Mass192.042 Da
Topological Polar Surface Area63.600 Ų
Heavy Atom Count14
Formal Charge0
Complexity216.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Kun Yuan, Kehuai Feng, Sheng Liao, Xiaoning Liao, Yichen Zou, Dan Hou, Xuliang Nie, Wanming Xiong.  (2023)  Synthesis, characterization, and electrochemical properties of phenyl-coupled diimidazolium hexafluorophosphate ionic liquids.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2023.123515]
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.